| Term Name: | spermatogenic failure 11 |
|---|---|
| Synonyms: | SPGF11 |
| Definition: | A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21. |
| Ontology: | Human Disease [DOID:0070180] ( DOID:0070180 ) |